(Associate) Medical Director - Neurology

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Discover Impactful Work : The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department. A day in the Life : Provide medical leadership to the study teams, including creating clinical trial protocols, implementing the latest scientific information, contributing to site selection, and reviewing and approving study protocols, amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviations, and other clinical documents. Real-time Medical Monitoring of clinical studies: ensure medical validity of primary endpoints and study subject safety, identify medical issues early, and address concerns proactively in consultation with the Global Medical Indication Lead. Review protocols, support staff regarding procedural and budgetary items, and manage protocol amendments. Serve as the chief liaison between the sponsor and internal departments, ensuring effective communication and issue resolution. Educate investigator sites and handle day-to-day activities during clinical trials. Act as the medical point of contact for stakeholders: interact with investigators, respond to IRBs and Health Authorities, prepare and present material to safety committees, and provide medical training at investigator meetings and for CRAs. Ensure study compliance with SOPs and GCP guidelines. Collaborate closely with cross-functional study team members to clarify medical risks, issues, and results. Education : MD, MB/BS or equivalent degree with strong medical knowledge, preferably with clinical experience in neurology. Knowledge, Skills, Abilities : Extensive experience in the pharmaceutical industry, clinical trials, and pharmaceutical medicine. Fluency in spoken and written English. Understanding of NDA submission processes and regulatory guidelines for adverse event reporting. Strong communication and presentation skills, a team player. Apply today! Thermo Fisher Scientific is an EEO / Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. J-18808-Ljbffr

Location: ibiza, ES

Posted Date: 5/12/2025